Dietrich A, Mitchison N A, Rajnavölgyi E, Schneider S C
Deutsches Rheuma ForschungsZentrum Berlin, Germany.
J Autoimmun. 1994 Oct;7(5):601-9. doi: 10.1006/jaut.1994.1044.
A central question in understanding autoimmunity is whether an endogenous self-antigen can drive an immune response initially triggered by a foreign one. This possibility is here tested by adoptive transfer, in which T and B cells from mice primed with foreign type II collagen were transferred into irradiated syngeneic hosts. Previous work with other protein antigens has established that primed cells normally respond only if boosted after transfer with antigen. In the present case, and in respect only to that portion of the antibody response able to bind to endogenous type II collagen, that requirement did not hold. This indicates that the anti-self component is indeed driven by endogenous antigen, which the transferred lymphocytes presumably obtain from their adoptive hosts. The transfers were carried out in C57BL10.A x DBA/1 mice using donors primed with either chick or bovine collagen, and the non-boosted responses, presumably driven by endogenous antigen, could be followed in a proportion of the recipients for as long as 45 days.
理解自身免疫的一个核心问题是内源性自身抗原是否能够驱动最初由外源性抗原引发的免疫反应。在此通过过继转移来检验这种可能性,即将用外源性II型胶原致敏的小鼠的T细胞和B细胞转移到经辐射的同基因宿主中。先前针对其他蛋白质抗原的研究已经证实,致敏细胞通常只有在转移后用抗原进行增强刺激时才会产生反应。在本研究中,仅就能够结合内源性II型胶原的那部分抗体反应而言,这一要求并不成立。这表明抗自身成分确实是由内源性抗原驱动的,而转移的淋巴细胞大概是从其受体宿主获得这种内源性抗原的。转移实验是在C57BL10.A×DBA/1小鼠中进行的,使用用鸡或牛胶原致敏的供体,并且在一部分受体中可以追踪到长达45天的、大概由内源性抗原驱动的非增强反应。